Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2003. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
129114016 | Hereditary corneal dystrophy | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
818666013 | Hereditary corneal dystrophy (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary corneal dystrophy | Is a | Corneal dystrophy | true | Inferred relationship | Existential restriction modifier | ||
Hereditary corneal dystrophy | Finding site | Corneal structure | true | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary corneal dystrophy | Is a | Hereditary disorder of the visual system | true | Inferred relationship | Existential restriction modifier | ||
Hereditary corneal dystrophy | Associated morphology | Dystrophy | false | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary corneal dystrophy | Finding site | Corneal structure | false | Inferred relationship | Existential restriction modifier | 1 | |
Hereditary corneal dystrophy | Associated morphology | Dystrophy | true | Inferred relationship | Existential restriction modifier | 1 |
This concept is not in any reference sets